MNGIE, Mitochondrial neurogastrointestinal encephalopathy

CASE

MNGIE is a rare autosomal recessive mitochondrial disease. Gastrointestinal manifestation results in gastrointestinal dysmotility possibly resulting in pseudo-obstruction in which the muscular contractions become inefficient. This small bowel follow through shows atypical pattern of non-propulsive contractions of the intestine.

Radiology image - MNGIE, Mitochondrial neurogastrointestinal encephalopathy: Abdomen, Small bowel: RF - Fluoroscopy

MNGIE, Mitochondrial neurogastrointestinal encephalopathy


MNGIE, Mitochondrial neurogastrointestinal encephalopathy: RF - FluoroscopyMNGIE, Mitochondrial neurogastrointestinal encephalopathy: RF - FluoroscopyMNGIE, Mitochondrial neurogastrointestinal encephalopathy: RF - FluoroscopyMNGIE, Mitochondrial neurogastrointestinal encephalopathy: RF - FluoroscopyMNGIE, Mitochondrial neurogastrointestinal encephalopathy: RF - Fluoroscopy
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